• Benign Prostatic Hyperplasia;
  • Erectile Dysfunction;
  • Infertility;
  • Phosphodiesterase;
  • Sexual Dysfunction;
  • Sildenafil;
  • Tadalafil;
  • Urinary Incontinence;
  • Vardenafil;
  • Vinpocetine

Conflict of Interest. Francesco Montorsi: Consultant for Pfizer Inc, GSK, Lilly Icos, Bayer, and AMS. Jackie Corbin: Supported by NIH DK40029 and DK58277; speaker for Pfizer Inc. and Bayer/GSK; research support from ICOS and Bayer. Stephen Phillips: Employee of Pfizer Inc., and investment interest (stock holder and share options).


Introduction.  With the success of Phosphodiesterase (PDE) type 5 inhibitors (i.e., sildenafil, tadalafil, vardenafil) in the treatment of erectile dysfunction (ED), PDEs are considered attractive targets for drug intervention in the urogenital tract.

Aim.  To review the role of PDEs, which exist as a superfamily of enzymes comprising 11 distinct families, in the urogenital system, focusing on anatomical locations, functions and dysfunctions, potential disorders that could be treated, and any promising new selective PDE inhibitors under development.

Methods.  Included are (i) abstracts from 2001, 2002, and 2003; (ii) a MEDLINE search from 1996 through December 2003; and (iii) a pipeline search for therapeutics in development. Data from animal experiments are presented when there is a paucity of human data, but with the caveat that the distribution of PDE isozymes in a specific tissue can vary between species.

Results.  PDE mRNA and protein have been localized throughout the normal human urogenital tract. Double-blind, placebo-controlled studies suggest possible new clinical roles for sildenafil, including prophylaxis to preserve penile smooth muscle and erectile function after radical prostatectomy, and treatment of ejaculatory delay secondary to serotonergic reuptake inhibitor antidepressant therapy. Open-label studies suggest a potential clinical role for: vinpocetine (a PDE1 inhibitor) in the treatment of incontinence and low-compliance bladder; and sildenafil in the treatment of premature ejaculation, prostate-related lower urinary tract symptoms, and in women who have had unsuccessful in vitro fertilization. Several new orally administered PDE5 inhibitors are in early clinical development for the treatment of ED. Potential indications for PDE inhibitors that are suggested by preclinical data include Peyronie's disease, ureteral colic, male and female birth control, and prevention of preterm labor.

Conclusions.  Drug selectivity and differential PDE tissue distribution allow for potential targeted intervention for numerous disorders related to the urogenital tract.